{"title":"大气压下冰熔点附近CO2与环戊烷和乙基环己烷水合物的保存","authors":"Motoi Oshima*, , , Satoshi Takeya, , , Yusuke Jin, , , Kiyofumi Suzuki, , and , Jiro Nagao, ","doi":"10.1021/acs.energyfuels.5c02959","DOIUrl":null,"url":null,"abstract":"<p >In this study, we investigated the preservation of CO<sub>2</sub> hydrates in organic liquids near the melting point of ice at atmospheric pressure under isothermal temperature conditions to enable CO<sub>2</sub> storage and transportation using gas hydrates under milder temperature and pressure conditions. Cyclopentane (CP), ethylcyclohexane (ECH), and 2-ethyl-1-hexanol (2-EH) were used as organic liquids and their effects on the dissociation behaviors of the CO<sub>2</sub> hydrate were evaluated. After 24 h, the preservation ratios of CO<sub>2</sub> hydrate powders with CP or ECH were ∼70% at 265 K and ∼60% at 269 K. In contrast, the preservation ratios without organic liquids were ∼30% at 265 K and ∼10% at 269 K. The analysis revealed that CP promoted the formation of CP hydrate shells on the CO<sub>2</sub> hydrate surface during dissociation, whereas ECH facilitated ice shell formation. However, the CO<sub>2</sub> hydrate with 2-EH dissociated rapidly within approximately 1 h at 265 and 269 K because 2-EH inhibited ice shell formation. These results indicate that hydrophobic CP and ECH enhance the CO<sub>2</sub> hydrate stability by enabling the formation of shell structures by CP hydrate or ice that encapsulates the hydrates and prevents CO<sub>2</sub> gas release.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 40","pages":"19342–19349"},"PeriodicalIF":5.3000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preservation of CO2 Hydrates with Cyclopentane and Ethylcyclohexane near the Melting Point of Ice under Atmospheric Pressure\",\"authors\":\"Motoi Oshima*, , , Satoshi Takeya, , , Yusuke Jin, , , Kiyofumi Suzuki, , and , Jiro Nagao, \",\"doi\":\"10.1021/acs.energyfuels.5c02959\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In this study, we investigated the preservation of CO<sub>2</sub> hydrates in organic liquids near the melting point of ice at atmospheric pressure under isothermal temperature conditions to enable CO<sub>2</sub> storage and transportation using gas hydrates under milder temperature and pressure conditions. Cyclopentane (CP), ethylcyclohexane (ECH), and 2-ethyl-1-hexanol (2-EH) were used as organic liquids and their effects on the dissociation behaviors of the CO<sub>2</sub> hydrate were evaluated. After 24 h, the preservation ratios of CO<sub>2</sub> hydrate powders with CP or ECH were ∼70% at 265 K and ∼60% at 269 K. In contrast, the preservation ratios without organic liquids were ∼30% at 265 K and ∼10% at 269 K. The analysis revealed that CP promoted the formation of CP hydrate shells on the CO<sub>2</sub> hydrate surface during dissociation, whereas ECH facilitated ice shell formation. However, the CO<sub>2</sub> hydrate with 2-EH dissociated rapidly within approximately 1 h at 265 and 269 K because 2-EH inhibited ice shell formation. These results indicate that hydrophobic CP and ECH enhance the CO<sub>2</sub> hydrate stability by enabling the formation of shell structures by CP hydrate or ice that encapsulates the hydrates and prevents CO<sub>2</sub> gas release.</p>\",\"PeriodicalId\":35,\"journal\":{\"name\":\"Energy & Fuels\",\"volume\":\"39 40\",\"pages\":\"19342–19349\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Fuels\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c02959\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c02959","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Preservation of CO2 Hydrates with Cyclopentane and Ethylcyclohexane near the Melting Point of Ice under Atmospheric Pressure
In this study, we investigated the preservation of CO2 hydrates in organic liquids near the melting point of ice at atmospheric pressure under isothermal temperature conditions to enable CO2 storage and transportation using gas hydrates under milder temperature and pressure conditions. Cyclopentane (CP), ethylcyclohexane (ECH), and 2-ethyl-1-hexanol (2-EH) were used as organic liquids and their effects on the dissociation behaviors of the CO2 hydrate were evaluated. After 24 h, the preservation ratios of CO2 hydrate powders with CP or ECH were ∼70% at 265 K and ∼60% at 269 K. In contrast, the preservation ratios without organic liquids were ∼30% at 265 K and ∼10% at 269 K. The analysis revealed that CP promoted the formation of CP hydrate shells on the CO2 hydrate surface during dissociation, whereas ECH facilitated ice shell formation. However, the CO2 hydrate with 2-EH dissociated rapidly within approximately 1 h at 265 and 269 K because 2-EH inhibited ice shell formation. These results indicate that hydrophobic CP and ECH enhance the CO2 hydrate stability by enabling the formation of shell structures by CP hydrate or ice that encapsulates the hydrates and prevents CO2 gas release.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.